
501 - 1000 employees
Founded 1984
đł Fintech
đ¤ B2B
đŚ Banking
Fintech ⢠B2B ⢠Banking
Rho is a financial technology company that provides integrated banking solutions for businesses, combining modern banking with cash management and expense tracking. Their platform focuses on streamlining financial operations and offering a user-friendly interface for better control of company finances.
đ April 21
đşđ¸ United States â Remote
đľ $80k - $108k / year
â° Full Time
đĄ Mid-level
đ Senior
đ˛ Risk
đŚ H1B Visa Sponsor
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501 - 1000 employees
Founded 1984
đł Fintech
đ¤ B2B
đŚ Banking
Fintech ⢠B2B ⢠Banking
Rho is a financial technology company that provides integrated banking solutions for businesses, combining modern banking with cash management and expense tracking. Their platform focuses on streamlining financial operations and offering a user-friendly interface for better control of company finances.
⢠Manages project-level RBQM activities and documents for multiple projects ⢠Facilitates and leads study-specific risk assessments and suggests appropriate anticipated risks and mitigations ⢠Reviews and understands protocol, critical data and process, safety, and data integrity risks related to protocol execution ⢠Ensures project teams develop an integrated quality risk management strategy in compliance with ICH E6R3 guidelines ⢠Participates in ongoing RBQM process and tool optimization activities ⢠Develops and maintains Integrated Quality Risk Management Plan (IQRMP) and Quality Risk Log for assigned studies in coordination with cross functional team ⢠Documents observations and actionable items noted during reviews; investigates trends, issues, and risks for root cause ⢠Documents completion of activities via tracking, reporting, and/or other required project documents as per SOP ⢠Reviews and understands protocol, critical data and process, safety, and data integrity risks related to protocol execution ⢠Reviews study and site data listings and visualizations to identify trends, risks, potential or suspected scientific misconduct, or other systematic errors that could impact data integrity and subject safety ⢠Immediately communicates and escalates serious issues to the relevant project team member(s) and, with guidance, develops action plans ⢠Initiates set-up and provides inputs needed for Key Risk Indicator (KRI) visualizations, using either a technology platform or an alternate tool ⢠Applies knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes ⢠Keeps up with industry trends, including changes to regulations or standard practices ⢠Ensures adherence to compliance standards across all RBQM activities ⢠For assigned activities, understands project scope, budgets, and timelines; manages study activities to ensure project objectives, deliverables, and timelines are met ⢠Attends sponsor kick-off meetings and may attend Investigator Meetings. ⢠Participates in project staff meetings as applicable ⢠Coordinates and manages cross-functional activities and responsibilities for assigned study teams ⢠Collaborates with study team management to define and enforce compliance with Rho RBQM processes and contracted activities ⢠Attends clinical training sessions according to the project-specific requirements ⢠May support training and mentoring of Associate QRM ⢠Supports internal and sponsor audits and participates in efforts to ensure readiness ⢠Identifies opportunities for process improvements and communicates to RBQM leadership
⢠Bachelor Degree in science or a related field ⢠3 years of industry experience ⢠Applicable experience in one or more of the following in a clinical research setting: clinical monitoring, data management, biostatistics, or related function; and/or at least 1 year of strong performance in an AQRM role ⢠Sound knowledge of Good Clinical Practice/ICH E6 (R3) Guidelines, Risk-Based Monitoring strategies, processes and tools and/or other applicable regulatory requirements and industry trends ⢠Basic knowledge of clinical data collection, monitoring, and review processes ⢠Solid understanding of the entire clinical data lifecycle, from protocol creation through database lock and analysis ⢠Able to quickly adapt to changing priorities to achieve goals/targets ⢠Able to assess and implement protocol-specific Quality Management approaches as needed, while collaborating with the appropriate impacted functions. ⢠Ability to maintain confidentiality ⢠Proactively takes initiative to identify next steps, issues, or gaps, and drive tasks forward with minimal guidance ⢠Ability to set priorities and manage multiple projects within moderate oversight ⢠Ability to work independently, prioritize responsibilities, and work in a team environment ⢠Demonstrates strong computer skills and is able to embrace new technologies ⢠Strong competency with MS Excel functionality (sorting, filtering, calculations, pivot tables) ⢠Proficiency with Analytical Data Visualization Tools ⢠Demonstrates the ability to think critically, problem solve and apply sound judgment and reasoning for assigned tasks ⢠Communicates clearly and professionally in written and verbal formats with both internal and external stakeholders, translating moderate-to-complex concepts into clear, actionable messages ⢠Solid presentation skills, both written and spoken, with an ability to inform, influence, convince, and persuade ⢠Expected required travel 15% on average
⢠Rho provides a comprehensive benefits package for all benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k). ⢠All employees are eligible for paid time off, holidays, parental leave and bereavement leave. ⢠We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives outside work.
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